US9472804B2 - Anodes comprising germanium for lithium-ion devices - Google Patents

Anodes comprising germanium for lithium-ion devices Download PDF

Info

Publication number
US9472804B2
US9472804B2 US14/926,012 US201514926012A US9472804B2 US 9472804 B2 US9472804 B2 US 9472804B2 US 201514926012 A US201514926012 A US 201514926012A US 9472804 B2 US9472804 B2 US 9472804B2
Authority
US
United States
Prior art keywords
weight
anode material
germanium
anode
total weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
US14/926,012
Other versions
US20160141612A1 (en
Inventor
Doron Burshtain
Ronny Costi
Carmit OPHIR
Daniel Aronov
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Storedot Ltd
Original Assignee
Storedot Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Storedot Ltd filed Critical Storedot Ltd
Priority to US14/926,012 priority Critical patent/US9472804B2/en
Priority to EP15192846.2A priority patent/EP3024067B1/en
Priority to CN201510772042.1A priority patent/CN105609748B/en
Priority to KR1020150161083A priority patent/KR102413376B1/en
Assigned to StoreDot Ltd. reassignment StoreDot Ltd. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: COSTI, RONNY, ARONOV, DANIEL, BURSHTAIN, Doron, OPHIR, CARMIT
Publication of US20160141612A1 publication Critical patent/US20160141612A1/en
Priority to US15/263,399 priority patent/US9728776B2/en
Priority to US15/264,641 priority patent/US9583761B2/en
Priority to US15/271,234 priority patent/US9871247B2/en
Publication of US9472804B2 publication Critical patent/US9472804B2/en
Application granted granted Critical
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/38Selection of substances as active materials, active masses, active liquids of elements or alloys
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/04Hybrid capacitors
    • H01G11/06Hybrid capacitors with one of the electrodes allowing ions to be reversibly doped thereinto, e.g. lithium ion capacitors [LIC]
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/08Structural combinations, e.g. assembly or connection, of hybrid or EDL capacitors with other electric components, at least one hybrid or EDL capacitor being the main component
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22Electrodes
    • H01G11/30Electrodes characterised by their material
    • H01G11/50Electrodes characterised by their material specially adapted for lithium-ion capacitors, e.g. for lithium-doping or for intercalation
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/52Separators
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/54Electrolytes
    • H01G11/56Solid electrolytes, e.g. gels; Additives therein
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/54Electrolytes
    • H01G11/58Liquid electrolytes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/74Terminals, e.g. extensions of current collectors
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/052Li-accumulators
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/052Li-accumulators
    • H01M10/0525Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/056Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
    • H01M10/0565Polymeric materials, e.g. gel-type or solid-type
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/056Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
    • H01M10/0566Liquid materials
    • H01M10/0569Liquid materials characterised by the solvents
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/13Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/133Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/13Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/134Electrodes based on metals, Si or alloys
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/13Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/136Electrodes based on inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/362Composites
    • H01M4/364Composites as mixtures
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/38Selection of substances as active materials, active masses, active liquids of elements or alloys
    • H01M4/386Silicon or alloys based on silicon
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/58Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/583Carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • H01M4/587Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/621Binders
    • H01M4/622Binders being polymers
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/621Binders
    • H01M4/622Binders being polymers
    • H01M4/623Binders being polymers fluorinated polymers
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/624Electric conductive fillers
    • H01M4/625Carbon or graphite
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M2004/026Electrodes composed of, or comprising, active material characterised by the polarity
    • H01M2004/027Negative electrodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2220/00Batteries for particular applications
    • H01M2220/20Batteries in motive systems, e.g. vehicle, ship, plane
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2220/00Batteries for particular applications
    • H01M2220/30Batteries in portable systems, e.g. mobile phone, laptop
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409Separators, membranes or diaphragms characterised by the material
    • H01M50/411Organic material
    • H01M50/414Synthetic resins, e.g. thermoplastics or thermosetting resins
    • H01M50/417Polyolefins
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Definitions

  • the present disclosure relates to electrode active materials used in lithium ion devices, such as rechargeable lithium ion batteries.
  • Lithium ion batteries also known as Li-ion Batteries or LIB's are widely used in consumer electronics, for example in mobile telephones, tablets and laptops. LIB's are also used in other fields, such as military uses, electric vehicles and aerospace applications.
  • Li-ions lithium ions
  • energy is used to transfer the Li-ions back to the high-energy anode assembly.
  • the charge and discharge processes in batteries are slow processes, and can degrade the chemical compounds inside the battery over time. Rapid charging causes accelerated degradation of the battery constituents, as well as a potential fire hazard due to a localized, over-potential build-up and increased heat generation—which can ignite the internal components, and lead to explosion.
  • An anode material for a lithium ion device may include an active material including germanium and boron.
  • the weight percentage of the germanium may be between about 5 to 80 weight % of the total weight of the anode material and the weight percentage of the boron may be between about 2 to 20 weight % of the total weight of the anode material.
  • the weight percentage of the germanium may be between about 60 to about 75 weight % of the total weight of the anode material and the weight percentage of the boron may be between about 3 to about 6 weight % of the total weight of the anode material.
  • An active material for producing anodes for Li-ion devices may include germanium at a weight percentage of about between 6.5 to 94 weight % of the total weight of the active material and boron at a weight percentage of about between 1.5 to 15 weight % of the total weight of the active material.
  • the active material may include carbon.
  • the active material may further include tungsten at a weight percentage of between about 6 to about 25 weight % tungsten of the total weight of the active material.
  • the lithium ion device may include an anode having an active material comprising germanium and boron.
  • the weight percentage of the germanium may be between about 5 to 80 weight % of the total weight of the anode and the weight percentage of the boron may be between about 2 to 20 weight % of the total weight of the anode.
  • the lithium ion device may further include a cathode and an electrolyte.
  • Some embodiments of the invention may be directed to a method for making an anode material for a lithium ion device.
  • the method may include forming an alloy from germanium powder, carbon, and a boron-containing compound to form an active material, and adding the active material to a matrix to form the anode material.
  • the weight percentage of the germanium is between about 5 to about 80 weight % of the total weight of the anode material and the weight percentage of the boron is between about 2 to about 20 weight % of the total weight of the anode material.
  • FIG. 1 is an illustration of an exemplary lithium ion device according to some embodiments of the invention.
  • FIG. 2 is a graph presenting first-cycle charge-discharge curves of an exemplary lithium-ion half-cell for a germanium-based anode containing boron and tungsten according to some embodiments of the invention.
  • FIG. 3 is a graph presenting charge-discharge graph as a function of the cycle for a germanium-based anode containing boron and tungsten according to some embodiments of the invention.
  • the active material may include an alloy comprising graphite (C), germanium (Ge) and boron (B).
  • the carbon, germanium and boron may be milled together to form an alloy. Other methods for forming alloys may be used.
  • the active material may further include silicon (Si) and tungsten (W) in the form of tungsten carbide (WC) particles.
  • the active material may include an alloy comprising graphite (C), germanium (Ge) and tungsten (W).
  • alloy includes an intimate mixture of metal powders, as described above.
  • the weight percentage of the germanium may be between about 5 to 80 weight % of the total weight of the anode material and the weight percentage of the boron may be between about 2 to 20 weight % of the total weight of the anode material.
  • the anode material may further include tungsten. The percentage of the tungsten may be between about 2 to 20 weight % of the total weight of the anode material.
  • the weight percentage of the germanium may be between about 60 to 75 weight % of the total weight of the anode material
  • the weight percentage of the boron may be between about 3 to 6 weight % of the total weight of the anode material.
  • the weight percentage of the carbon (in the form of graphite) within the active material may be between about 0.5 to 5 weight % of the total weight of the anode material.
  • the weight percentage of the tungsten may be between 7 to about 11 weight % of the total weight of the anode material.
  • the active material within the anode material may further include silicon.
  • the amount of silicon is added such that the weight ratio between the germanium and the silicon is at least 4 to 1, for example, 5 to 1, 6 to 1 or more.
  • An exemplary anode material having 60 weight % germanium of the total weight of the anode material may include 12 weight % silicon of the total weight of the anode material.
  • q>0and z 0.
  • r 0 .
  • the compound further includes: (b) micro-particles and/or nano-particles, wherein the micro-particles and/or the nano-particles are particles of at least one type selected from the group consisting of: amorphous, crystalline, polycrystalline, any physical form of the formula, a metal carbide of the formula, a metal borat, boron, an organometallic compound, and a pre-prepared alloy of the formula in any physical form.
  • a lithium ion device 100 may include an anode 110 as detailed herein, a cathode 120 and an electrolyte 130 suitable for lithium ion devices.
  • a non-limiting list of exemplary lithium ion devices may be Li-ion batteries, Li-ion capacitors and Li-ion hybrid system including both a battery and a capacitor.
  • Electrolyte 130 may be in the form of a liquid, solid or gel. Examples of solid electrolytes include polymeric electrolytes such as polyethylene oxide, fluorine-containing polymers and copolymers (e.g., polytetrafluoroethylene), and combinations thereof.
  • liquid electrolytes examples include ethylene carbonate, diethyl carbonate, propylene carbonate, fluoroethylene carbonate (FEC), and combinations thereof.
  • the electrolyte may be provided with a lithium electrolyte salt.
  • suitable salts include LiPF 6 , LiBF 4 , lithium bis(oxalato)borate, LiN(CF 3 SO 2 ) 2 , LiN(C 2 F 5 SO 2 ) 2 , LiAsF 6 , LiC(CF 3 SO 2 ) 3 , LiClO 4 , and LiTFSI.
  • Cathode 120 may include cathode compositions suitable for the use in lithium ion devices. Examples of suitable cathode compositions may include LiCoO 2 , LiCo 0.33 Mn 0.33 Ni 0.33 O 2 , LiMn 2 O 4 , and LiFePO 4 .
  • lithium ion device 100 may further include a separator (not illustrated).
  • the separator may be configured to separate between the anode and the cathode.
  • An exemplary separator according to some embodiments of the invention may include poly ethylene (PE), polypropylene (PP) or the like.
  • Anode 110 according to embodiments of the invention when incorporated in a lithium ion device, such as battery, exhibits improved cycle-life and coulombic efficiency over common anodes.
  • the mechanical stability of the anode (achieved after the first cycle, or after several initial cycles), and hence of the lithium ion device, is also improved.
  • Such stability is assumed to be attributed to the incorporation of the tungsten and/or boron into the expanding germanium-lithium alloy during the charge-discharge process.
  • Such incorporation may help prevent metallization of the lithium during charging due to the relatively strong lithium-tungsten and/or lithium-boron binding. Such strong binding may result in a partly-charged assembly which may contribute to the enhanced stability and cycle life of the anode.
  • boron and/or tungsten may facilitate the electrochemical utilization of the germanium (and the silicon in a Si—Ge anode material), and substantially may reduce the migration of germanium into the electrode substrate.
  • boron carbide may enhance the binding energy of Li atoms, (boron's binding energy is greater than the cohesive energy of lithium metal) and may prevent lithium from clustering at high lithium doping concentrations.
  • Lithium ions may react with boron carbide and germanium oxide to form lithium carbide, lithium boride, lithium oxide and mainly lithium tetraborate, thus leaving the Li ions partly charged.
  • Such partial surface charges in Li—Ge—C alloys may stabilize the overall structure externally and/or internally.
  • External stabilization may occur as a result of preventing lithium metallization by keeping the lithium as a tetraborate salt.
  • Internal stabilization may occur as a result of leaving the internal germanium alloy structure with ⁇ + centers, and hence providing a stable matrix for lithium ion transport inside the germanium structure, during the extraction and insertion of lithium ions.
  • Tungsten carbide with naturally-occurring germanium oxide-carbon composites may improve the electrochemical behavior of the anode.
  • the tungsten-carbide may act as hydron (H + ) ion bather.
  • Tungsten carbide is highly conductive and inert substance, therefore, may further stabilize the conductivity of the electrode over the life cycle and therefore, may stabilize the conductivity of the electrode.
  • Preparation of the anode may include milling and/or mixing processes.
  • a germanium powder and graphite powder may be inserted into a high-energy ball-miller to be milled under protective atmosphere or non-protective atmosphere.
  • a boron-carbide (B 4 C) powder may be added to the pre-milled Ge/C mixture inside the miller.
  • Si powder may further be added to the Ge/C mixture inside the miller.
  • the miller may include hardened alumina media that may be agitated at 1000-1500 RPM.
  • the milling stage may produce an alloy having nano-size particles of around 20-100 nm particle size.
  • an emulsion containing nano-sized tungsten carbide (WC) particles may be added to the as milled powder (Ge/C or Ge/C/B alloy) at the end of the milling process to produce the active material for the anode.
  • the tungsten carbide particle size may be between around 20 to 60 nm.
  • nano-sized particles means particles having an average particle size less than one micron, in embodiments “nano-sized” means particles having an average particle size less than 100 nm.
  • the active material for making anodes for Li-ions devices may include a germanium-carbon-boron-tungsten alloy, a germanium-carbon-boron alloy, germanium-silicon-carbon-boron alloy or a germanium-carbon-tungsten alloy. Additional polymeric binders and conductive additives may be added to the alloy to form the final anode material.
  • An exemplary anode may include conductive materials at a weight percentage of about between 5 to 10 weight % of the total weight of the anode material and binder material at a weight percentage of about between 0.01 to 5 weight % of the total weight of the anode material.
  • Exemplary conductive elements may include spherical carbon, carbon nano-tubes and/or graphene particles.
  • the active material may include a germanium-carbon-boron alloy, in which the weight percentage of the germanium may be between about 6.5 to about 94 weight % of the total weight of the active material, the weight percentage of the boron may be between about 1.5 to about 15 weight % of the total weight of the active material and the weight percentage of the carbon may be between about 6.5 to about 25 weight % of the total weight of the active material.
  • the active material may further include tungsten and/or silicon. The weight percentage of the tungsten may be between 8-30 weight % of the total weight of the active material and the silicon may be added such that the weight ratio between the germanium and the silicon is at least 4 to 1.
  • the active material may include a germanium-carbon-boron-tungsten alloy, in which the weight percentage of the germanium may be between about 72 to about 96 weight % of the total weight of the active material, the weight percentage of the boron may be between about 3 to about 6 weight % of the total weight of the active material, the weight percentage of the carbon may be between about 0.66 to about 6.6 weight % of the total weight of the active material. In some embodiments, when the active material includes tungsten, the weight percentage of the tungsten may be between about 6 to 25 weight % of the total weight of the active material.
  • the active material may include a germanium-carbon-tungsten alloy, in which the weight percentage of the germanium may be between about 6.5 to about 94 weight % of the total weight of the active material, the weight percentage of the carbon may be between about 0.67 to about 6.7 weight % of the total weight of the active material and the weight percentage of the tungsten may be between about 6 to about 25 weight % of the total weight of the active material.
  • the anode material may further include carbon nano-tubes (CNT) at a weight percentage of about between 0.05 to 0.5 weight % of the total weight of the anode.
  • the carbon nano-tubes may replace the tungsten carbide particles or be added to the anode material in addition to the tungsten carbide particles.
  • the alloy material may include between 0.06-0.8 weight % carbon nano-tubes of the total weight of the anode material.
  • An exemplary anode material may include 0.1-0.3 weight % single-rod carbon nano-tubes.
  • FIG. 2 presenting first-cycle charge-discharge curves of an exemplary lithium-ion half-cell for a germanium-based anode containing boron and tungsten according to some embodiments of the invention.
  • the voltage of the half-cell is presented as a function of the charge values in mAh/g.
  • the exemplary anode material included (in weight percentage from the total weight of the anode) 69% Ge, 3% C, 10% W, 5% B, 10% binder and 3% conductive additives (Ge 0.69 C 0.03 W 0.10 B 0.050 Binder 0.1 ConductiveAditive 0.03 ).
  • the as-milled Ge/C/W/B alloy i.e.
  • the active material included 79% Ge, 3% C, 12% W and 6% B weight percent of the total weight of the alloy (Ge 0.79 C 0.03 W 0.12 B 0.06 ).
  • the first-cycle efficiency is defined as the first discharge yield divided by the first charge yield.
  • the first charge capacity is much higher than the theoretical first charge capacity of 1,143 mAh/g known for germanium. This behavior is probably due to the reaction between available lithium ions and boron and/or tungsten, as explained above.
  • FIG. 3 presenting charge-discharge graph as a function of the cycle for a germanium-based anode containing boron and tungsten according to some embodiments of the invention.
  • the same type of half-cell with the same anode that was tested to create the graph presented in FIG. 2 was used again in a multi cycle charge-discharge tests.
  • At the first 6 cycles there is a drop in capacitance that may be attributed to the expansion/contraction of the germanium particles.
  • the anode stabilized, resulting in a very high coulombic efficiency (99%) and a stable cyclic response.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Power Engineering (AREA)
  • Materials Engineering (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Manufacturing & Machinery (AREA)
  • Inorganic Chemistry (AREA)
  • Composite Materials (AREA)
  • General Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • Physics & Mathematics (AREA)
  • Dispersion Chemistry (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

An anode material for a lithium ion device includes an active material including germanium and boron. The weight percentage of the germanium is between about 45 to 80 weight % of the total weight of the anode material and the weight percentage of the boron is between about 2 to 20 weight % of the total weight of the anode material. The active material may include carbon at a weight percentage of between 0.5 to about 5 weight % of the total weight of the anode material. Additional materials, methods of making and devices are taught.

Description

CROSS REFERENCE TO RELATED APPLICATIONS
This application claims the benefit of U.S. Provisional Application Ser. No. 62/081,043, filed on Nov. 18, 2014 and entitled “COMPOUNDS FOR BATTERY ELECTRODES, ENERGY-STORAGE DEVICES, AND METHODS THEREIN”, which is incorporated in its entirety herein by reference.
BACKGROUND OF THE INVENTION
The present disclosure relates to electrode active materials used in lithium ion devices, such as rechargeable lithium ion batteries.
Lithium ion batteries, also known as Li-ion Batteries or LIB's are widely used in consumer electronics, for example in mobile telephones, tablets and laptops. LIB's are also used in other fields, such as military uses, electric vehicles and aerospace applications. During discharge of the battery, lithium ions (Li-ions) travel from a high-energy anode material through an electrolyte and a separator to a low-energy cathode material. During charging, energy is used to transfer the Li-ions back to the high-energy anode assembly. The charge and discharge processes in batteries are slow processes, and can degrade the chemical compounds inside the battery over time. Rapid charging causes accelerated degradation of the battery constituents, as well as a potential fire hazard due to a localized, over-potential build-up and increased heat generation—which can ignite the internal components, and lead to explosion.
Typical Li-ion battery anodes contain mostly graphite. Silicon or germanium, as anode-alloying components, generally exhibit higher lithium absorption capacities in comparison to anodes containing only graphite. Such silicon-containing or germanium-containing electrodes, however, usually exhibit poor life cycle and poor coulombic efficiency due to the mechanical expansion of silicon and germanium upon alloying with lithium, and upon lithium extraction from the alloy, which reduce the silicon alloy volume. Such mechanical instability results in the material breaking into fragments.
SUMMARY OF THE INVENTION
Some embodiments of the invention may be directed to lithium-ion devices and in particular to anodes for lithium-ion devices. An anode material for a lithium ion device according to some embodiments of the invention may include an active material including germanium and boron. In some embodiments, the weight percentage of the germanium may be between about 5 to 80 weight % of the total weight of the anode material and the weight percentage of the boron may be between about 2 to 20 weight % of the total weight of the anode material. In some embodiments, the weight percentage of the germanium may be between about 60 to about 75 weight % of the total weight of the anode material and the weight percentage of the boron may be between about 3 to about 6 weight % of the total weight of the anode material.
An active material for producing anodes for Li-ion devices may include germanium at a weight percentage of about between 6.5 to 94 weight % of the total weight of the active material and boron at a weight percentage of about between 1.5 to 15 weight % of the total weight of the active material. In some embodiments, the active material may include carbon. In some embodiments, the active material may further include tungsten at a weight percentage of between about 6 to about 25 weight % tungsten of the total weight of the active material.
Some embodiments of the invention may be directed to a lithium ion device. The lithium ion device may include an anode having an active material comprising germanium and boron. In some embodiments, the weight percentage of the germanium may be between about 5 to 80 weight % of the total weight of the anode and the weight percentage of the boron may be between about 2 to 20 weight % of the total weight of the anode. The lithium ion device may further include a cathode and an electrolyte.
Some embodiments of the invention may be directed to a method for making an anode material for a lithium ion device. The method may include forming an alloy from germanium powder, carbon, and a boron-containing compound to form an active material, and adding the active material to a matrix to form the anode material. In some embodiments, the weight percentage of the germanium is between about 5 to about 80 weight % of the total weight of the anode material and the weight percentage of the boron is between about 2 to about 20 weight % of the total weight of the anode material.
BRIEF DESCRIPTION OF THE DRAWINGS
The subject matter regarded as the invention is particularly pointed out and distinctly claimed in the concluding portion of the specification. The invention, however, both as to organization and method of operation, together with objects, features, and advantages thereof, may best be understood by reference to the following detailed description when read with the accompanying drawings in which:
FIG. 1 is an illustration of an exemplary lithium ion device according to some embodiments of the invention;
FIG. 2 is a graph presenting first-cycle charge-discharge curves of an exemplary lithium-ion half-cell for a germanium-based anode containing boron and tungsten according to some embodiments of the invention; and
FIG. 3 is a graph presenting charge-discharge graph as a function of the cycle for a germanium-based anode containing boron and tungsten according to some embodiments of the invention.
It will be appreciated that for simplicity and clarity of illustration, elements shown in the figures have not necessarily been drawn to scale. For example, the dimensions of some of the elements may be exaggerated relative to other elements for clarity. Further, where considered appropriate, reference numerals may be repeated among the figures to indicate corresponding or analogous elements.
DETAILED DESCRIPTION OF THE PRESENT INVENTION
In the following detailed description, numerous specific details are set forth in order to provide a thorough understanding of the invention. However, it will be understood by those skilled in the art that the present invention may be practiced without these specific details. In other instances, well-known methods, procedures, and components have not been described in detail so as not to obscure the present invention.
Embodiments of the invention describe anodes for lithium ion devices, an active material (anode intercalation compounds) for manufacturing the anodes and the lithium ion devices. The term active material refers herein to an alloying material that is chemically active with lithium ions. The lithium ion devices may include lithium ion batteries (Li-ion battery or LIB), Li-ion capacitors (LIC), Li-ion hybrid system including both a battery and a capacitor or the like.
The active material may include an alloy comprising graphite (C), germanium (Ge) and boron (B). The carbon, germanium and boron may be milled together to form an alloy. Other methods for forming alloys may be used. In some embodiments, the active material may further include silicon (Si) and tungsten (W) in the form of tungsten carbide (WC) particles. In some embodiments, the active material may include an alloy comprising graphite (C), germanium (Ge) and tungsten (W). As used herein, “alloy” includes an intimate mixture of metal powders, as described above.
According to embodiments of the invention, the composition of the anode may comprise an active anode material as detailed herein, a binder and/or plasticizer (e.g. polyvinylidene fluoride (PVDF)) and a conductive agent (e.g. carbon black and carbon-nano-tubes (CNT)).
According to some embodiments, the weight percentage of the germanium may be between about 5 to 80 weight % of the total weight of the anode material and the weight percentage of the boron may be between about 2 to 20 weight % of the total weight of the anode material. According to other embodiments, the anode material may further include tungsten. The percentage of the tungsten may be between about 2 to 20 weight % of the total weight of the anode material.
In some embodiments, the weight percentage of the germanium may be between about 60 to 75 weight % of the total weight of the anode material, the weight percentage of the boron may be between about 3 to 6 weight % of the total weight of the anode material. The weight percentage of the carbon (in the form of graphite) within the active material may be between about 0.5 to 5 weight % of the total weight of the anode material. In some embodiments, the weight percentage of the tungsten may be between 7 to about 11 weight % of the total weight of the anode material.
In some embodiments, the active material within the anode material may further include silicon. The amount of silicon is added such that the weight ratio between the germanium and the silicon is at least 4 to 1, for example, 5 to 1, 6 to 1 or more. An exemplary anode material having 60 weight % germanium of the total weight of the anode material may include 12 weight % silicon of the total weight of the anode material.
According to the present invention, there is provided a compound for forming electrodes, the compound including: (a) a general formula of Gex,SiyCpBqWz,Nr, wherein x, y, p, q, z, and r represent normalized weight ratios in which approximately 0.1≦x≦1, 0≦y≦0.20, 0≦q≦0.20, 0≦z≦0.20, lq-zl>0, 0≦r≦0.10, and x+y+q+p+z +r=1.00. Preferably, wherein q>0and z=0. Most preferably, wherein r=0. Preferably, wherein q=0 and z>0. Most preferably, wherein r=0. Preferably, wherein q=0 and z>0.Most preferably, wherein r=0. Preferably, wherein q>0 and z>0. Most preferably, wherein r=0.
Preferably, the compound further includes: (b) micro-particles and/or nano-particles, wherein the micro-particles and/or the nano-particles are particles of at least one type selected from the group consisting of: amorphous, crystalline, polycrystalline, any physical form of the formula, a metal carbide of the formula, a metal borat, boron, an organometallic compound, and a pre-prepared alloy of the formula in any physical form.
Reference is made to FIG. 1, illustrating an exemplary lithium ion device according to some embodiments of the invention. A lithium ion device 100 may include an anode 110 as detailed herein, a cathode 120 and an electrolyte 130 suitable for lithium ion devices. A non-limiting list of exemplary lithium ion devices may be Li-ion batteries, Li-ion capacitors and Li-ion hybrid system including both a battery and a capacitor. Electrolyte 130 may be in the form of a liquid, solid or gel. Examples of solid electrolytes include polymeric electrolytes such as polyethylene oxide, fluorine-containing polymers and copolymers (e.g., polytetrafluoroethylene), and combinations thereof. Examples of liquid electrolytes include ethylene carbonate, diethyl carbonate, propylene carbonate, fluoroethylene carbonate (FEC), and combinations thereof. The electrolyte may be provided with a lithium electrolyte salt. Examples of suitable salts include LiPF6, LiBF4, lithium bis(oxalato)borate, LiN(CF3SO2)2, LiN(C2F5SO2)2, LiAsF6, LiC(CF3SO2)3, LiClO4, and LiTFSI. Cathode 120 may include cathode compositions suitable for the use in lithium ion devices. Examples of suitable cathode compositions may include LiCoO2, LiCo0.33Mn0.33Ni0.33O2, LiMn2O4, and LiFePO4.
In some embodiments, lithium ion device 100 may further include a separator (not illustrated). The separator may be configured to separate between the anode and the cathode. An exemplary separator according to some embodiments of the invention may include poly ethylene (PE), polypropylene (PP) or the like.
Anode 110 according to embodiments of the invention, when incorporated in a lithium ion device, such as battery, exhibits improved cycle-life and coulombic efficiency over common anodes. The mechanical stability of the anode (achieved after the first cycle, or after several initial cycles), and hence of the lithium ion device, is also improved. Such stability is assumed to be attributed to the incorporation of the tungsten and/or boron into the expanding germanium-lithium alloy during the charge-discharge process. Such incorporation may help prevent metallization of the lithium during charging due to the relatively strong lithium-tungsten and/or lithium-boron binding. Such strong binding may result in a partly-charged assembly which may contribute to the enhanced stability and cycle life of the anode.
The presence of boron and/or tungsten may facilitate the electrochemical utilization of the germanium (and the silicon in a Si—Ge anode material), and substantially may reduce the migration of germanium into the electrode substrate. Moreover, boron carbide may enhance the binding energy of Li atoms, (boron's binding energy is greater than the cohesive energy of lithium metal) and may prevent lithium from clustering at high lithium doping concentrations.
Boron carbide, which is inert to oxidation at the anode in the electrochemical reaction, interacts with germanium, germanium oxide and lithium. Lithium ions may react with boron carbide and germanium oxide to form lithium carbide, lithium boride, lithium oxide and mainly lithium tetraborate, thus leaving the Li ions partly charged. Such partial surface charges in Li—Ge—C alloys may stabilize the overall structure externally and/or internally. External stabilization may occur as a result of preventing lithium metallization by keeping the lithium as a tetraborate salt. Internal stabilization may occur as a result of leaving the internal germanium alloy structure with δ+ centers, and hence providing a stable matrix for lithium ion transport inside the germanium structure, during the extraction and insertion of lithium ions.
Tungsten carbide with naturally-occurring germanium oxide-carbon composites may improve the electrochemical behavior of the anode. The tungsten-carbide may act as hydron (H+) ion bather. Tungsten carbide is highly conductive and inert substance, therefore, may further stabilize the conductivity of the electrode over the life cycle and therefore, may stabilize the conductivity of the electrode.
Preparation of the anode may include milling and/or mixing processes. In some embodiments, a germanium powder and graphite powder may be inserted into a high-energy ball-miller to be milled under protective atmosphere or non-protective atmosphere. In some embodiments, a boron-carbide (B4C) powder may be added to the pre-milled Ge/C mixture inside the miller. In some embodiments, Si powder may further be added to the Ge/C mixture inside the miller. The miller may include hardened alumina media that may be agitated at 1000-1500 RPM. The milling stage may produce an alloy having nano-size particles of around 20-100 nm particle size. In some embodiments, an emulsion containing nano-sized tungsten carbide (WC) particles may be added to the as milled powder (Ge/C or Ge/C/B alloy) at the end of the milling process to produce the active material for the anode. The tungsten carbide particle size may be between around 20 to 60 nm. As used herein, “nano-sized” particles means particles having an average particle size less than one micron, in embodiments “nano-sized” means particles having an average particle size less than 100 nm.
The active material for making anodes for Li-ions devices (e.g., device 100), such as batteries may include a germanium-carbon-boron-tungsten alloy, a germanium-carbon-boron alloy, germanium-silicon-carbon-boron alloy or a germanium-carbon-tungsten alloy. Additional polymeric binders and conductive additives may be added to the alloy to form the final anode material. An exemplary anode, according to embodiments of the invention, may include conductive materials at a weight percentage of about between 5 to 10 weight % of the total weight of the anode material and binder material at a weight percentage of about between 0.01 to 5 weight % of the total weight of the anode material. Exemplary conductive elements may include spherical carbon, carbon nano-tubes and/or graphene particles.
In some embodiments, the active material may include a germanium-carbon-boron alloy, in which the weight percentage of the germanium may be between about 6.5 to about 94 weight % of the total weight of the active material, the weight percentage of the boron may be between about 1.5 to about 15 weight % of the total weight of the active material and the weight percentage of the carbon may be between about 6.5 to about 25 weight % of the total weight of the active material. In some embodiments, the active material may further include tungsten and/or silicon. The weight percentage of the tungsten may be between 8-30 weight % of the total weight of the active material and the silicon may be added such that the weight ratio between the germanium and the silicon is at least 4 to 1.
In some embodiments, the active material may include a germanium-carbon-boron-tungsten alloy, in which the weight percentage of the germanium may be between about 72 to about 96 weight % of the total weight of the active material, the weight percentage of the boron may be between about 3 to about 6 weight % of the total weight of the active material, the weight percentage of the carbon may be between about 0.66 to about 6.6 weight % of the total weight of the active material. In some embodiments, when the active material includes tungsten, the weight percentage of the tungsten may be between about 6 to 25 weight % of the total weight of the active material. In some embodiments, the active material may include a germanium-carbon-tungsten alloy, in which the weight percentage of the germanium may be between about 6.5 to about 94 weight % of the total weight of the active material, the weight percentage of the carbon may be between about 0.67 to about 6.7 weight % of the total weight of the active material and the weight percentage of the tungsten may be between about 6 to about 25 weight % of the total weight of the active material.
In some embodiments, the anode material may further include carbon nano-tubes (CNT) at a weight percentage of about between 0.05 to 0.5 weight % of the total weight of the anode. The carbon nano-tubes may replace the tungsten carbide particles or be added to the anode material in addition to the tungsten carbide particles. Accordingly, the alloy material may include between 0.06-0.8 weight % carbon nano-tubes of the total weight of the anode material. An exemplary anode material may include 0.1-0.3 weight % single-rod carbon nano-tubes.
EXAMPLES
Reference is made to FIG. 2 presenting first-cycle charge-discharge curves of an exemplary lithium-ion half-cell for a germanium-based anode containing boron and tungsten according to some embodiments of the invention. The voltage of the half-cell is presented as a function of the charge values in mAh/g. The exemplary anode material included (in weight percentage from the total weight of the anode) 69% Ge, 3% C, 10% W, 5% B, 10% binder and 3% conductive additives (Ge0.69C0.03W0.10B0.050Binder0.1ConductiveAditive0.03). The as-milled Ge/C/W/B alloy (i.e. the active material) included 79% Ge, 3% C, 12% W and 6% B weight percent of the total weight of the alloy (Ge0.79C0.03W0.12B0.06). Looking at the graphs of FIG. 2, the first charge yielded 1,705 mAh/g, and the discharge produced 913 mAh/g, resulting in a 53.5% first-cycle efficiency. The first-cycle efficiency is defined as the first discharge yield divided by the first charge yield. The first charge capacity is much higher than the theoretical first charge capacity of 1,143 mAh/g known for germanium. This behavior is probably due to the reaction between available lithium ions and boron and/or tungsten, as explained above.
Reference is made to FIG. 3, presenting charge-discharge graph as a function of the cycle for a germanium-based anode containing boron and tungsten according to some embodiments of the invention. The same type of half-cell with the same anode that was tested to create the graph presented in FIG. 2 was used again in a multi cycle charge-discharge tests. At the first 6 cycles there is a drop in capacitance that may be attributed to the expansion/contraction of the germanium particles. However, already after 7 cycles the anode stabilized, resulting in a very high coulombic efficiency (99%) and a stable cyclic response.
While certain features of the invention have been illustrated and described herein, many modifications, substitutions, changes, and equivalents will now occur to those of ordinary skill in the art. It is, therefore, to be understood that the appended claims are intended to cover all such modifications and changes as fall within the true spirit of the invention.

Claims (7)

The invention claimed is:
1. An anode material for a lithium ion device, comprising:
an active material comprising germanium nano-particles having a particle size of 20 to 100 nm, boron carbide nano-particles having a particle size of 20 to 100 nm and tungsten carbide nano-particles having a particle size of 20 to 60 nm, wherein the weight percentage of the germanium is between 5 to 80 weight % of the total weight of the anode material, the weight percentage of boron in the anode material is between 2 to 20 weight % of the total weight of the anode material and the weight percentage of tungsten in the anode material is between 5 to 20 weight % of the total weight of the anode material.
2. The anode material of claim 1, wherein the active material further comprises carbon at a weight percentage of between 0.5 to 5 weight % of the total weight of the anode material.
3. The anode material of claim 1, wherein the active material further comprises silicon and a weight ratio of germanium to silicon in the active material is at least 4 to 1.
4. The anode material of claim 1, wherein the weight percentage of the germanium is between 60 to 75 weight % of the total weight of the anode material and the weight percentage of the boron in the anode material is between 3 to 6 weight % of the total weight of the anode material.
5. The anode material of claim 1, wherein the weight percentage of the tungsten in the anode material is between 7 to 11 weight % of the total weight of the anode material.
6. The anode material of claim 1, further comprising:
one or more conductive materials, wherein the weight percentage of the conductive materials is between 0.01 to 5 weight % of the total weight of the anode material.
7. The anode material of claim 1, further comprising:
a binder at a weight percentage of between 0.1 to 10 weight % of the total weight of the anode material.
US14/926,012 2014-11-18 2015-10-29 Anodes comprising germanium for lithium-ion devices Active US9472804B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
US14/926,012 US9472804B2 (en) 2014-11-18 2015-10-29 Anodes comprising germanium for lithium-ion devices
EP15192846.2A EP3024067B1 (en) 2014-11-18 2015-11-03 Compounds for battery electrodes, energy storage devices, and methods
CN201510772042.1A CN105609748B (en) 2014-11-18 2015-11-12 Anode for lithium ion device including germanium
KR1020150161083A KR102413376B1 (en) 2014-11-18 2015-11-17 Compounds for battery electrodes, energy storage devices, and methods
US15/263,399 US9728776B2 (en) 2014-11-18 2016-09-13 Germanium-containing lithium-ion devices
US15/264,641 US9583761B2 (en) 2014-11-18 2016-09-14 Methods for making anodes for germanium-containing lithium-ion devices
US15/271,234 US9871247B2 (en) 2014-11-18 2016-09-21 Germanium-containing active material for anodes for lithium-ion devices

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201462081043P 2014-11-18 2014-11-18
US14/926,012 US9472804B2 (en) 2014-11-18 2015-10-29 Anodes comprising germanium for lithium-ion devices

Related Child Applications (3)

Application Number Title Priority Date Filing Date
US15/263,399 Division US9728776B2 (en) 2014-11-18 2016-09-13 Germanium-containing lithium-ion devices
US15/264,641 Division US9583761B2 (en) 2014-11-18 2016-09-14 Methods for making anodes for germanium-containing lithium-ion devices
US15/271,234 Division US9871247B2 (en) 2014-11-18 2016-09-21 Germanium-containing active material for anodes for lithium-ion devices

Publications (2)

Publication Number Publication Date
US20160141612A1 US20160141612A1 (en) 2016-05-19
US9472804B2 true US9472804B2 (en) 2016-10-18

Family

ID=54366090

Family Applications (4)

Application Number Title Priority Date Filing Date
US14/926,012 Active US9472804B2 (en) 2014-11-18 2015-10-29 Anodes comprising germanium for lithium-ion devices
US15/263,399 Active US9728776B2 (en) 2014-11-18 2016-09-13 Germanium-containing lithium-ion devices
US15/264,641 Active US9583761B2 (en) 2014-11-18 2016-09-14 Methods for making anodes for germanium-containing lithium-ion devices
US15/271,234 Active US9871247B2 (en) 2014-11-18 2016-09-21 Germanium-containing active material for anodes for lithium-ion devices

Family Applications After (3)

Application Number Title Priority Date Filing Date
US15/263,399 Active US9728776B2 (en) 2014-11-18 2016-09-13 Germanium-containing lithium-ion devices
US15/264,641 Active US9583761B2 (en) 2014-11-18 2016-09-14 Methods for making anodes for germanium-containing lithium-ion devices
US15/271,234 Active US9871247B2 (en) 2014-11-18 2016-09-21 Germanium-containing active material for anodes for lithium-ion devices

Country Status (4)

Country Link
US (4) US9472804B2 (en)
EP (1) EP3024067B1 (en)
KR (1) KR102413376B1 (en)
CN (1) CN105609748B (en)

Cited By (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20160380258A1 (en) * 2014-11-18 2016-12-29 StoreDot Ltd. Germanium-containing lithium-ion devices
EP3336937A1 (en) 2016-12-15 2018-06-20 StoreDot Ltd. Electric vehicles with adaptive fast-charging, utilizing supercapacitor-emulating batteries
US10096859B2 (en) 2016-04-07 2018-10-09 StoreDot Ltd. Electrolytes with ionic liquid additives for lithium ion batteries
US10110036B2 (en) 2016-12-15 2018-10-23 StoreDot Ltd. Supercapacitor-emulating fast-charging batteries and devices
US10199646B2 (en) 2014-07-30 2019-02-05 StoreDot Ltd. Anodes for lithium-ion devices
US10199677B2 (en) 2016-04-07 2019-02-05 StoreDot Ltd. Electrolytes for lithium ion batteries
US10290864B2 (en) 2016-04-07 2019-05-14 StoreDot Ltd. Coated pre-lithiated anode material particles and cross-linked polymer coatings
US10293704B2 (en) 2014-04-08 2019-05-21 StoreDot Ltd. Electric vehicles with adaptive fast-charging, utilizing supercapacitor-emulating batteries
US10355271B2 (en) 2016-04-07 2019-07-16 StoreDot Ltd. Lithium borates and phosphates coatings
US10367191B2 (en) 2016-04-07 2019-07-30 StoreDot Ltd. Tin silicon anode active material
US10367192B2 (en) 2016-04-07 2019-07-30 StoreDot Ltd. Aluminum anode active material
US10403889B2 (en) 2014-10-21 2019-09-03 RAMOT AT TEL-AVIV UNlVERSITY LTD. High-capacity silicon nanowire based anode for lithium-ion batteries
US10454101B2 (en) 2017-01-25 2019-10-22 StoreDot Ltd. Composite anode material made of core-shell particles
US10468727B2 (en) 2016-04-07 2019-11-05 StoreDot Ltd. Graphite-carbohydrate active material particles with carbonized carbohydrates
US10549650B2 (en) 2014-04-08 2020-02-04 StoreDot Ltd. Internally adjustable modular single battery systems for power systems
US10581065B1 (en) 2019-01-28 2020-03-03 StoreDot Ltd. Production of metalloid-based anodes for lithium ion batteries using dry etching
US10586977B1 (en) 2019-01-23 2020-03-10 StoreDot Ltd. Electrodes made of electrically conductive metallic porous structure with embedded active material particles
US10608463B1 (en) 2019-01-23 2020-03-31 StoreDot Ltd. Direct charging of battery cell stacks
US10818919B2 (en) 2016-04-07 2020-10-27 StoreDot Ltd. Polymer coatings and anode material pre-lithiation
US10862104B2 (en) 2019-01-28 2020-12-08 StoreDot Ltd. Mono-cell batteries
US10916811B2 (en) 2016-04-07 2021-02-09 StoreDot Ltd. Semi-solid electrolytes with flexible particle coatings
US11128152B2 (en) 2014-04-08 2021-09-21 StoreDot Ltd. Systems and methods for adaptive fast-charging for mobile devices and devices having sporadic power-source connection
US11205796B2 (en) 2016-04-07 2021-12-21 StoreDot Ltd. Electrolyte additives in lithium-ion batteries
US11264810B2 (en) 2019-03-21 2022-03-01 StoreDot Ltd. Balancing charging of lithium ion batteries by a switching circuitry
US11495835B2 (en) 2019-03-06 2022-11-08 StoreDot Ltd. Management of large stacks of battery cells
US11569499B2 (en) 2019-01-23 2023-01-31 StoreDot Ltd. Aerogel-based electrodes
US11658279B2 (en) 2020-01-07 2023-05-23 StoreDot Ltd. Method for configuring and prelithiating a fast charging cell
US11831012B2 (en) 2019-04-25 2023-11-28 StoreDot Ltd. Passivated silicon-based anode material particles

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110380036B (en) * 2019-07-24 2022-04-12 福州大学 Alloy material composite carbon nanotube and preparation method and application thereof
RU2743576C1 (en) * 2020-08-12 2021-02-20 Федеральное государственное бюджетное учреждение науки Институт физической химии и электрохимии им. А.Н. Фрумкина Российской академии наук (ИФХЭ РАН) Anode of lithium-ion battery for operation at lower temperatures and method for producing it
KR102416184B1 (en) * 2020-08-26 2022-07-05 경상국립대학교산학협력단 Super capacitor electrode material and manufacturing method thereof
US11901564B2 (en) 2022-02-09 2024-02-13 Socpra Sciences Et Génie S.E.C. Anisotropic porous germanium nanostructures achieved with fast bipolar electrochemical etching and chemical etching

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3778254A (en) 1971-11-18 1973-12-11 Atomic Energy Commission Brazing filler metal for molybdenum
US20020146623A1 (en) * 1998-09-11 2002-10-10 Kimihito Suzuki Lithium secondary battery and active material for negative electrode in lithium secondary battery
US20040219428A1 (en) 2003-05-01 2004-11-04 Nissan Motor Co., Ltd. High-speed charging/discharging electrode and battery
US7192673B1 (en) * 1999-10-22 2007-03-20 Sanyo Electric Co., Ltd. Electrode for rechargeable lithium battery and rechargeable lithium battery
US20090179181A1 (en) * 2008-01-11 2009-07-16 A123 Systems, Inc. Silicon based composite material
US20100190059A1 (en) * 2004-04-22 2010-07-29 Graetz Jason A High-capacity nanostructured germanium-containing materials and lithium alloys thereof
US20110257001A1 (en) 2010-04-15 2011-10-20 Hoya Corporation Optical glass, preform for precision press molding, optical element, and method for manufacturing optical element
US20130260285A1 (en) 2010-12-09 2013-10-03 Nhk Spring Co., Ltd. Brazing material for bonding in atmosphere, bonded article, and current collecting material

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW431002B (en) * 1998-09-11 2001-04-21 Nippon Steel Corp Lithium secondary battery and active material for negative electrode in lithium secondary battery
JP4940571B2 (en) * 2005-04-08 2012-05-30 ソニー株式会社 Lithium ion secondary battery
CN101728513B (en) * 2009-12-03 2012-07-04 武汉大学 Compound for anode material of lithium ion secondary battery and preparation method thereof
JP5623783B2 (en) * 2010-05-13 2014-11-12 日本発條株式会社 Brazing material for air bonding, bonded body, and current collecting material
JP6006662B2 (en) * 2013-03-05 2016-10-12 信越化学工業株式会社 Method for producing silicon-containing particles, method for producing negative electrode material for non-aqueous electrolyte secondary battery, and method for producing non-aqueous electrolyte secondary battery
US9472804B2 (en) * 2014-11-18 2016-10-18 StoreDot Ltd. Anodes comprising germanium for lithium-ion devices

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3778254A (en) 1971-11-18 1973-12-11 Atomic Energy Commission Brazing filler metal for molybdenum
US20020146623A1 (en) * 1998-09-11 2002-10-10 Kimihito Suzuki Lithium secondary battery and active material for negative electrode in lithium secondary battery
US7192673B1 (en) * 1999-10-22 2007-03-20 Sanyo Electric Co., Ltd. Electrode for rechargeable lithium battery and rechargeable lithium battery
US20040219428A1 (en) 2003-05-01 2004-11-04 Nissan Motor Co., Ltd. High-speed charging/discharging electrode and battery
US20100190059A1 (en) * 2004-04-22 2010-07-29 Graetz Jason A High-capacity nanostructured germanium-containing materials and lithium alloys thereof
US20090179181A1 (en) * 2008-01-11 2009-07-16 A123 Systems, Inc. Silicon based composite material
US20110257001A1 (en) 2010-04-15 2011-10-20 Hoya Corporation Optical glass, preform for precision press molding, optical element, and method for manufacturing optical element
US20130260285A1 (en) 2010-12-09 2013-10-03 Nhk Spring Co., Ltd. Brazing material for bonding in atmosphere, bonded article, and current collecting material

Non-Patent Citations (9)

* Cited by examiner, † Cited by third party
Title
Bin Wang et al. "The Dimensionality of Sn Anodes in Li Ion Batteries" Materials Today Dec. 2012 | vol. 15 | No. 12 pp. 544-552.
D. R. Secrist "Compound Formation in the Systems Lithium-Carbon and Lithium-Boron" Journal of the American Ceramic Society vol. 50, No. 10 pp. 520-523 Oct. 1967.
European Serach Report from European Application No. EP 15 19 2846 dated Jan. 12, 2016.
Jee Ho Yom et al. "Improved electrochemical behavior of Tungsten coated Silicon monoxide-Carbon composite anode in lithium ion battery" Abstract #1041, 224th ECS Meeting, © 2013 The Electrochemical Society.
Kennedy et al. "Nanowire Heterostructures Comprising Germanium Stems and Silicon Branches as High-Capacity Li-Ion Anodes with Tunable Rate Capability" ACS Nano 2015 9 (7), 7456-7465. *
Li-Feng Cui et al. "Carbon-Silicon Core-Shell Nanowires as High Capacity Electrode for Lithium Ion Batteries" Nano Letters 2009; vol. 9, No. 9 pp. 3370-3374 Received May 27, 2009; Revised Manuscript Received Jul. 2, 2009.
Naoki Suzuki et al. "Silicon nitride thin film electrode for lithium-ion batteries" Journal of Power Sources 231 (2013) pp. 186-189.
Tadhg Kennedy et al. "Nanowire Heterostructures Comprising Germanium Stems and Silicon Branches as High-Capacity Li-Ion Anodes with Tunable Rate Capability" Jul. 6, 2015 ASC NANO Published online 10.1021/ascnano.5b02528.
Xiaojun Wu et al. "Hydrogen Storage in Pillared Li-Dispersed Boron Carbide Nanotubes" J. Phys. Chem. C 2008, 112, pp. 8458-8463 Received: Oct. 15, 2007; Revised Manuscript Received: Mar. 18, 2008.

Cited By (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10293704B2 (en) 2014-04-08 2019-05-21 StoreDot Ltd. Electric vehicles with adaptive fast-charging, utilizing supercapacitor-emulating batteries
US11560062B2 (en) 2014-04-08 2023-01-24 StoreDot Ltd. Software management of EV battery modules
US11128152B2 (en) 2014-04-08 2021-09-21 StoreDot Ltd. Systems and methods for adaptive fast-charging for mobile devices and devices having sporadic power-source connection
US10549650B2 (en) 2014-04-08 2020-02-04 StoreDot Ltd. Internally adjustable modular single battery systems for power systems
US10199646B2 (en) 2014-07-30 2019-02-05 StoreDot Ltd. Anodes for lithium-ion devices
US10403889B2 (en) 2014-10-21 2019-09-03 RAMOT AT TEL-AVIV UNlVERSITY LTD. High-capacity silicon nanowire based anode for lithium-ion batteries
US20170012279A1 (en) * 2014-11-18 2017-01-12 StoreDot Ltd. Germanium-containing active material for anodes for lithium-ion devices
US9728776B2 (en) * 2014-11-18 2017-08-08 StoreDot Ltd. Germanium-containing lithium-ion devices
US9871247B2 (en) * 2014-11-18 2018-01-16 StoreDot Ltd. Germanium-containing active material for anodes for lithium-ion devices
US20160380258A1 (en) * 2014-11-18 2016-12-29 StoreDot Ltd. Germanium-containing lithium-ion devices
US10355271B2 (en) 2016-04-07 2019-07-16 StoreDot Ltd. Lithium borates and phosphates coatings
US10818919B2 (en) 2016-04-07 2020-10-27 StoreDot Ltd. Polymer coatings and anode material pre-lithiation
US10367191B2 (en) 2016-04-07 2019-07-30 StoreDot Ltd. Tin silicon anode active material
US10367192B2 (en) 2016-04-07 2019-07-30 StoreDot Ltd. Aluminum anode active material
US10367193B2 (en) 2016-04-07 2019-07-30 StoreDot Ltd. Methods of preparing anodes using tin as active material
US10199677B2 (en) 2016-04-07 2019-02-05 StoreDot Ltd. Electrolytes for lithium ion batteries
US10424814B2 (en) 2016-04-07 2019-09-24 StoreDot Ltd. Introducing a mobile layer of ionic liquid into electrolytes of lithium ion batteries
US11594757B2 (en) 2016-04-07 2023-02-28 StoreDot Ltd. Partly immobilized ionic liquid electrolyte additives for lithium ion batteries
US10454104B2 (en) 2016-04-07 2019-10-22 StoreDot Ltd. Methods for preparing anodes from anode active material particles with lithium borates and phosphates coatings
US10461323B2 (en) 2016-04-07 2019-10-29 StoreDot Ltd. Composite lithium borates and/or phosphates and polymer coatings for active material particles
US10468727B2 (en) 2016-04-07 2019-11-05 StoreDot Ltd. Graphite-carbohydrate active material particles with carbonized carbohydrates
US11205796B2 (en) 2016-04-07 2021-12-21 StoreDot Ltd. Electrolyte additives in lithium-ion batteries
US10096859B2 (en) 2016-04-07 2018-10-09 StoreDot Ltd. Electrolytes with ionic liquid additives for lithium ion batteries
US11069918B2 (en) 2016-04-07 2021-07-20 StoreDot Ltd. Carbonate electrolytes for lithium ion batteries
US10923712B2 (en) 2016-04-07 2021-02-16 StoreDot Ltd. Preparing anodes for lithium ion cells from aluminum anode active material particles
US10916811B2 (en) 2016-04-07 2021-02-09 StoreDot Ltd. Semi-solid electrolytes with flexible particle coatings
US10680289B2 (en) 2016-04-07 2020-06-09 StoreDot Ltd. Buffering zone for preventing lithium metallization on the anode of lithium ion batteries
US10290864B2 (en) 2016-04-07 2019-05-14 StoreDot Ltd. Coated pre-lithiated anode material particles and cross-linked polymer coatings
US10910671B2 (en) 2016-04-07 2021-02-02 StoreDot Ltd. Mobile layer of ionic liquid in electrolytes
US10903530B2 (en) 2016-04-07 2021-01-26 StoreDot Ltd. Anode material particles with porous carbon-based shells
EP3336937A1 (en) 2016-12-15 2018-06-20 StoreDot Ltd. Electric vehicles with adaptive fast-charging, utilizing supercapacitor-emulating batteries
US10873200B2 (en) 2016-12-15 2020-12-22 StoreDot Ltd. Devices and methods comprising supercapacitor-emulating fast-charging batteries
US10110036B2 (en) 2016-12-15 2018-10-23 StoreDot Ltd. Supercapacitor-emulating fast-charging batteries and devices
US11936035B2 (en) 2017-01-25 2024-03-19 StoreDot Ltd. Composite anode material made of ionic-conducting electrically insulating material
US10505181B2 (en) 2017-01-25 2019-12-10 StoreDot Ltd. Composite anode material made of ionic-conducting electrically insulating material
US10454101B2 (en) 2017-01-25 2019-10-22 StoreDot Ltd. Composite anode material made of core-shell particles
US10608463B1 (en) 2019-01-23 2020-03-31 StoreDot Ltd. Direct charging of battery cell stacks
US10586977B1 (en) 2019-01-23 2020-03-10 StoreDot Ltd. Electrodes made of electrically conductive metallic porous structure with embedded active material particles
US11569499B2 (en) 2019-01-23 2023-01-31 StoreDot Ltd. Aerogel-based electrodes
US10581065B1 (en) 2019-01-28 2020-03-03 StoreDot Ltd. Production of metalloid-based anodes for lithium ion batteries using dry etching
US11302908B2 (en) 2019-01-28 2022-04-12 StoreDot Ltd. Anode preparation system applying dry etching treatment to the anodes
US10862104B2 (en) 2019-01-28 2020-12-08 StoreDot Ltd. Mono-cell batteries
US11495835B2 (en) 2019-03-06 2022-11-08 StoreDot Ltd. Management of large stacks of battery cells
US11264810B2 (en) 2019-03-21 2022-03-01 StoreDot Ltd. Balancing charging of lithium ion batteries by a switching circuitry
US11831012B2 (en) 2019-04-25 2023-11-28 StoreDot Ltd. Passivated silicon-based anode material particles
US11658279B2 (en) 2020-01-07 2023-05-23 StoreDot Ltd. Method for configuring and prelithiating a fast charging cell

Also Published As

Publication number Publication date
US9871247B2 (en) 2018-01-16
EP3024067A1 (en) 2016-05-25
US20160380258A1 (en) 2016-12-29
CN105609748A (en) 2016-05-25
CN105609748B (en) 2020-08-18
US9728776B2 (en) 2017-08-08
US20170005330A1 (en) 2017-01-05
EP3024067B1 (en) 2018-04-25
KR20160059440A (en) 2016-05-26
US20160141612A1 (en) 2016-05-19
US20170012279A1 (en) 2017-01-12
US9583761B2 (en) 2017-02-28
KR102413376B1 (en) 2022-06-24

Similar Documents

Publication Publication Date Title
US9871247B2 (en) Germanium-containing active material for anodes for lithium-ion devices
US20160036045A1 (en) Anodes for lithium-ion devices
US10199646B2 (en) Anodes for lithium-ion devices
KR102543109B1 (en) Lithium secondary battery and method of manufacturing the same
US20160261002A1 (en) Solid-state multi-layer electrolyte, electrochemical cell and battery including the electrolyte, and method of forming same
JP5716093B2 (en) Positive electrode active material for lithium ion capacitor and method for producing the same
JP2010135329A (en) Cathode and lithium battery adopting this
JP2015122340A (en) Lithium secondary battery
CN101017915A (en) Nonaqueous electrolyte secondary battery
CN115799601A (en) Lithium ion battery
CN106716685B (en) Positive electrode for nonaqueous electrolyte secondary battery and nonaqueous electrolyte secondary battery using same
CN110800134B (en) Method for improving the life of lithium-sulfur batteries
CN106663780B (en) Positive electrode for nonaqueous electrolyte secondary battery and nonaqueous electrolyte secondary battery
KR101445019B1 (en) Anode active material, method for preparing the same, and secondary battery using the anode active material
KR20150046861A (en) Positive electrode for lithium-sulfur battery and method for preparing the same
JP2023077703A (en) Anode for lithium ion secondary battery and lithium ion secondary battery with the anode
JP2022544975A (en) Lithium-sulfur secondary battery capsule and lithium-sulfur secondary battery containing the same
KR102446269B1 (en) Lithium secondary battery
KR20110120018A (en) Anode active material, method of preparing the same, and anode and lithium battery containing the material
KR20150142735A (en) Method for preparing of carbon-coated nbo_2 as negative electrode material for lithium-ion secondary battery
CN114556617A (en) Lithium ion battery and method for producing a lithium ion battery
Subburaj et al. Investigation on high performance electrodes active materials for advanced lithium-ion rechargeable batteries
JP2018049770A (en) Lithium ion secondary battery
KR20170068130A (en) Rechargeable lithium battery
KR20160018039A (en) Cathod active material composition for magnesium rechargeable batteries and magnesium rechargeable batteries including the same

Legal Events

Date Code Title Description
AS Assignment

Owner name: STOREDOT LTD., ISRAEL

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:BURSHTAIN, DORON;COSTI, RONNY;OPHIR, CARMIT;AND OTHERS;SIGNING DATES FROM 20151021 TO 20151026;REEL/FRAME:037110/0570

STCF Information on status: patent grant

Free format text: PATENTED CASE

MAFP Maintenance fee payment

Free format text: PAYMENT OF MAINTENANCE FEE, 4TH YR, SMALL ENTITY (ORIGINAL EVENT CODE: M2551); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY

Year of fee payment: 4

MAFP Maintenance fee payment

Free format text: PAYMENT OF MAINTENANCE FEE, 8TH YR, SMALL ENTITY (ORIGINAL EVENT CODE: M2552); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY

Year of fee payment: 8